Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232524827G>A , CM000664.2:g.232524827G>A | GRCh38 |
| NC_000002.11:g.233389537G>A , CM000664.1:g.233389537G>A | GRCh37 |
| NC_000002.10:g.233097781G>A | NCBI36 |
| NG_008028.1:g.3616G>A | |
| NG_031969.1:g.9365G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001195129.2:c.1504G>A MANE Select | NP_001182058.1:p.Ala502Thr |
| ENST00000617714.2:c.1504G>A MANE Select | ENSP00000479745.1:p.Ala502Thr |
| NM_001195129.1:c.1504G>A | NP_001182058.1:p.Ala502Thr |
| NM_001369848.1:c.1507G>A | NP_001356777.1:p.Ala503Thr |
| ENST00000449534.6:c.1507G>A | ENSP00000473410.1:p.Ala503Thr |
| ENST00000617714.1:c.1504G>A | ENSP00000479745.1:p.Ala502Thr |